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Wellcome Trust Sanger Institute
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gi2017-vgp-poster Public
Scaling up reference quality assembly of vertebrate genomes
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minimap2 Public
Forked from lh3/minimap2A fast pairwise aligner for genomic and spliced nucleotide sequences
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www.htslib.org Public
Forked from samtools/www.htslib.orgThe http://www.htslib.org/ web site
HTML UpdatedOct 3, 2017 -
vgp-assembly Public
Forked from VGP/vgp-assemblyVGP repository for the genome assembly working group
UpdatedSep 22, 2017 -
capmq Public
Simple program to cap mapping quality in a given alignment file
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miniasm Public
Forked from lh3/miniasmUltrafast de novo assembly for long noisy reads (though having no consensus step)
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biogenomics-2017-vgp-poster Public
Plans for scaling vertebrate genome sequencing and assembly at the Sanger Institute
TeX UpdatedMar 14, 2017 -
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crumble Public
Forked from jkbonfield/crumbleExploration of controlled loss of quality values for compressing CRAM files
C UpdatedDec 14, 2016 -
freebayes Public
Forked from freebayes/freebayesBayesian haplotype-based polymorphism discovery and genotyping.
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Flexible genotype query among 30,000+ samples whole-genome
C MIT License UpdatedMay 6, 2016 -
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hapdip Public
Forked from lh3/hapdipThe CHM1-NA12878 benchmark for single-sample SNP/INDEL calling from WGS Illumina data
JavaScript UpdatedMay 26, 2015 -
bog_2015_poster Public
64,976 whole genome haplotypes from the Haplotype Reference Consortium and efficient algorithms to use them
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tools for working with variant graphs
C++ MIT License UpdatedMar 23, 2015 -
bgzeof Public
Detect truncation of BGZF files by checking the EOF marker exists
C MIT License UpdatedFeb 25, 2015 -
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Burrow-Wheeler Aligner for pairwise alignment between DNA sequences
C GNU General Public License v3.0 UpdatedDec 2, 2014 -
hrc-release1 Public
Setup for genotype likelihood calculation for the Haplotype Reference Consortium Release 1
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